Spinal Fusion Implant

ABSTRACT

An implant is described for anterior insertion in the spine. The implant includes a body and a cover, which house one or two blades attached to a blade actuating component. Each blade engages a corresponding channel in the blade actuating component. The blade or blades are extended or retracted when the blade actuating component is driven proximally inward or distally outward. Each blade is reinforced by a bridge portion formed along the distal facing side of the blade.

BACKGROUND

The embodiments are generally directed to implants for supporting bonegrowth in a patient.

A variety of different implants are used in the body. Implants used inthe body to stabilize an area and promote bone ingrowth provide bothstability (i.e. minimal deformation under pressure over time) and spacefor bone ingrowth.

Spinal fusion, also known as spondylodesis or spondylosyndesis, is asurgical treatment method used for the treatment of various morbiditiessuch as degenerative disc disease, spondylolisthesis (slippage of avertebra), spinal stenosis, scoliosis, fracture, infection or tumor. Theaim of the spinal fusion procedure is to reduce instability and thuspain.

In preparation for the spinal fusion, most of the intervertebral disc isremoved. An implant, the spinal fusion cage, may be placed between thevertebra to maintain spine alignment and disc height. The fusion (i.e.bone bridge) occurs between the endplates of the vertebrae.

SUMMARY

In one aspect, an implant includes a housing, where the housing has afirst axis, a blade, the blade having a retracted position in thehousing and an extended position where the blade extends outwardly fromthe housing, and a blade actuating component, where the blade actuatingcomponent includes a driven shaft portion and a blade engaging portion.The blade actuating component can move the blade between the retractedposition and the extended position. In addition, the housing includes afirst end, where the first end includes a guide opening, and the guideopening has a hollow grooved portion and a chamber portion. The hollowgrooved portion is connected to the chamber portion, and the chamberportion receives a portion of the driven shaft portion of the bladeactuating component.

In another aspect, an implant includes a body having a first axis, and ablade having a retracted position in the body and an extended positionwhere the blade extends outwardly from the body. The blade has a distalface and a proximal face. In addition, the blade has a bridge portiondisposed adjacent to the distal face, where the bridge portion isconfigured to provide structural reinforcement to the blade. The implantfurther includes a blade actuating component that can translate throughthe body in directions parallel to the first axis, and the bladeactuating component can move the blade between the retracted positionand the extended position.

In another aspect, an implant includes a housing, a first blade, and ablade actuating component. The first blade has a retracted position inthe housing and an extended position where the first blade extendsoutwardly from the housing. In addition, the blade actuating componentis configured to translate through the housing in directions parallel toa first axis, where the first axis extends from an anterior side of theimplant to a posterior side of the implant. The blade actuatingcomponent comprises a driven shaft portion and a blade engaging portion,the driven shaft portion being disposed at least partially outside ofthe housing when the first blade is the retracted position, and thedriven shaft portion being disposed entirely within the housing when thefirst blade is in the extended position.

Other systems, methods, features and advantages of the embodiments willbe, or will become, apparent to one of ordinary skill in the art uponexamination of the following figures and detailed description. It isintended that all such additional systems, methods, features andadvantages be included within this description and this summary, bewithin the scope of the embodiments, and be protected by the followingclaims.

BRIEF DESCRIPTION OF THE DRAWINGS

The embodiments can be better understood with reference to the followingdrawings and description. The components in the figures are notnecessarily to scale, with emphasis instead being placed uponillustrating the principles of the embodiments. Moreover, in thefigures, like reference numerals designate corresponding partsthroughout the different views.

FIG. 1 is a schematic view of a patient and an implant, according to anembodiment;

FIG. 2 is a schematic view of a patient and an implant with an insertiontool, according to an embodiment;

FIG. 3 is a schematic view of a spine and a deployed implant, accordingto an embodiment;

FIG. 4 is an isometric view of an embodiment of an implant;

FIG. 5 is an exploded isometric view of the implant of FIG. 4;

FIG. 6 is an isometric superior view of an embodiment of a body of animplant;

FIG. 7 is an isometric inferior view of an embodiment of a body of animplant;

FIG. 8 is a schematic posterior-side view of an embodiment of a body ofan implant;

FIG. 9 is a schematic anterior-side view of an embodiment of a body ofan implant;

FIG. 10 is a schematic isometric view of an embodiment of a bladeactuating component;

FIG. 11 is a schematic anterior-side view of an embodiment of a bladeactuating component;

FIG. 12 is a schematic side view of an embodiment of a blade actuatingcomponent;

FIG. 13 is a schematic isometric view of an embodiment of a blade;

FIG. 14 is a schematic isometric view of an embodiment of a blade;

FIG. 15 is a schematic view of an embodiment of a blade;

FIG. 16 is a schematic isometric view of an embodiment of a bladeactuating component and two corresponding blades;

FIG. 17 is a schematic isometric view of the blade actuating componentof FIG. 16 coupled with the two corresponding blades;

FIG. 18 is a schematic isometric view of a superior side of a cover ofan implant, according to an embodiment;

FIG. 19 is a schematic isometric view of an inferior side of the coverof FIG. 13;

FIG. 20 is a schematic isometric view of an embodiment of a body and acover for an implant;

FIG. 21 is a schematic isometric view of an embodiment of a body and acover for an implant;

FIG. 22 is a schematic isometric view of an implant in a deployedposition;

FIG. 23 is a schematic anterior-side view of an implant in a deployedposition;

FIG. 24 is a schematic lateral-side view of an implant in a deployedposition;

FIG. 25 is a schematic isometric view of an implant in an insertionposition, including a cross-sectional view of several components,according to an embodiment;

FIG. 26 is a schematic isometric view of the implant of FIG. 25 in anintermediate position between the insertion position and the deployedposition here, including a cross-sectional view of the severalcomponents;

FIG. 27 is a schematic isometric view of the implant of FIG. 25 in adeployed position, including a cross-sectional view of the severalcomponents;

FIG. 28 is a schematic isometric view of the implant of FIG. 25 in anintermediate position, including a cross-sectional view of the severalcomponents;

FIG. 29 is a schematic isometric view of a locking screw according to anembodiment;

FIG. 30 is a schematic side view of the locking screw of FIG. 29;

FIG. 31 is a schematic isometric view of an implant with a lockingscrew, according to an embodiment;

FIG. 32 is a schematic isometric view of an implant with a lockingscrew, according to an embodiment;

FIG. 33 is a schematic lateral-side view of a blade actuating componentfor an implant, according to another embodiment;

FIG. 34 is a cross-sectional view of an a body and a blade actuatingcomponent in the insertion position, according to another embodiment;

FIG. 35 is a cross-sectional view of an a body and a blade actuatingcomponent in the deployed position, according to another embodiment;

FIG. 36 is a schematic top-down view of an implant and an insertiontool; and

FIG. 37 is a schematic cross-sectional top-down view of the insertiontool with a representation of an implant of FIG. 36.

DETAILED DESCRIPTION

The embodiments described herein are directed to an implant for use in aspine. The embodiments include implants with a body and one or moreblades. In addition to the various provisions discussed below, anyembodiments may make use of any of the body/support structures, blades,actuating components or other structures disclosed in Duffield et al.,U.S. patent Ser. No. ______, published on ______, currently U.S. patentapplication Ser. No. 15/194,323, filed on Jun. 27, 2016 and titled“Interbody Fusion Device and System for Implantation,” Sack, U.S. patentSer. No. ______, published on ______, currently U.S. patent applicationSer. No. 15/296,902, filed on Oct. 18, 2016 and titled “Implant WithDeployable Blades,” and Duffield et al., U.S. patent Ser. No. ______,published on ______, currently U.S. patent application Ser. No.15/291,732, filed on Oct. 12, 2016 and titled “Insertion Tool ForImplant And Methods of Use,” each of which are hereby incorporated byreference in their entirety.

Introduction to the Implant

FIG. 1 is a schematic view of an embodiment of an implant 100. Forpurposes of context, implant 100 is shown adjacent to a depiction of aspinal column 102 in a human body 104. In FIG. 2, an embodiment ofimplant 100 is shown as it is being inserted into human body 104 withthe use of an insertion tool 206. It should be understood that therelative size of implant 100 and insertion tool 206 as depicted withhuman body 104 have been adjusted for purposes of illustration. Forpurposes of this disclosure, implant 100 may also be referred to as acage or fusion device. In some embodiments, implant 100 is configured tobe implanted within a portion of the human body. In some embodiments,implant 100 may be configured for implantation into the spine. In someembodiments, implant 100 may be a spinal fusion implant, or spinalfusion device, which is inserted between adjacent vertebrae to providesupport and/or facilitate fusion between the vertebrae. For example,referring to FIG. 3, a section of spinal column 102 is illustrated,where implant 100 has been positioned between a first vertebra 192 and asecond vertebra 194. Moreover, implant 100 is seen to include two blades(a first blade 241 and a second blade 242), which extend from thesuperior and inferior surfaces of implant 100. Each of the blades hasbeen driven into an adjacent vertebra (i.e., first vertebra 192 orsecond vertebra 194) so as to help anchor implant 100.

In some embodiments, implant 100 may be inserted using an anteriorlumbar interbody fusion (ALIF) surgical procedure, where the disc spaceis fused by approaching the spine through the abdomen. In the ALIFapproach, a three-inch to five-inch incision is typically made near theabdomen and the abdominal muscles are retracted to the side. In somecases, implant 100 can be inserted through a small incision in the frontor anterior side of the body. In some cases, an anterior approach mayafford improved exposure to the disc space to a surgeon. The anteriorapproach can allow a larger device to be used for the fusion, increasingthe surface area for a fusion to occur and allowing for morepostoperative stability. An anterior approach often makes it possible toreduce some of the deformity caused by various conditions, such asisthmic spondylolisthesis. Insertion and placement of the disc along thefront of a human body can also re-establish the patient's normalsagittal alignment in some cases, giving individuals a more normalinward curve to their low back.

For purposes of clarity, reference is made to various directionaladjectives throughout the detailed description and in the claims. Asused herein, the term “anterior” refers to a side or portion of animplant that is intended to be oriented towards the front of the humanbody when the implant has been placed in the body. Likewise, the term“posterior” refers to a side or portion of an implant that is intendedto be oriented towards the back of the human body followingimplantation. In addition, the term “superior” refers to a side orportion of an implant that is intended to be oriented towards a top(e.g., the head) of the body while “inferior” refers to a side orportion of an implant that is intended to be oriented towards a bottomof the body. Reference is also made herein to “lateral” sides orportions of an implant, which are sides or portions facing along alateral direction of the body.

FIG. 4 is a schematic isometric view of an embodiment of implant 100,according to an embodiment. As seen in FIG. 4, implant 100 is understoodto be configured with an anterior side 110 and a posterior side 112.Implant 100 may also include a first lateral side 114 and a secondlateral side 116. Furthermore, implant 100 may also include a superiorside 130 and an inferior side 140.

Reference is also made to directions or axes that are relative to theimplant itself, rather than to its intended orientation with regards tothe body. For example, the term “distal” refers to a part that islocated further from a center of an implant, while the term “proximal”refers to a part that is located closer to the center of the implant. Asused herein, the “center of the implant” could be the center of massand/or a central plane and/or another centrally located referencesurface.

An implant may also be associated with various axes. Referring to FIG.4, implant 100 may be associated with a longitudinal axis 120 thatextends along the longest dimension of implant 100 between first lateralside 114 and second lateral side 116. Additionally, implant 100 may beassociated with a posterior-anterior axis 122 (also referred to as a“widthwise axis”) that extends along the widthwise dimension of implant100, between posterior side 112 and anterior side 110. Moreover, implant100 may be associated with a vertical axis 124 that extends along thethickness dimension of implant 100 and which is generally perpendicularto both longitudinal axis 120 and posterior-anterior axis 122.

An implant may also be associated with various reference planes orsurfaces. As used herein, the term “median plane” refers to a verticalplane which passes from the anterior side to the posterior side of theimplant, dividing the implant into right and left halves, or lateralhalves. As used herein, the term “transverse plane” refers to ahorizontal plane located in the center of the implant that divides theimplant into superior and inferior halves. As used herein, the term“coronal plane” refers to a vertical plane located in the center of theimplant that divides the implant into anterior and posterior halves. Insome embodiments, the implant is symmetric or substantially symmetricabout two planes, such as the median and the transverse plane.

FIG. 5 is a schematic isometric exploded view of implant 100 accordingto an embodiment. Referring to FIGS. 4-5, implant 100 is comprised of abody 200 and a cover 220, which together may be referred to as a housing201 of implant 100. In some embodiments, a body and cover may beintegrally formed. In other embodiments, a body and cover may beseparate pieces that are joined by one or more fasteners. In theembodiment of FIGS. 4-5, body 200 and cover 220 are separate pieces thatare fastened together using additional components of implant 100.

Embodiments of an implant may include provisions for anchoring theimplant into adjacent vertebral bodies. In some embodiments, an implantmay include one or more anchoring members. In the embodiment of FIGS.4-5, implant 100 includes a set of blades 240 that facilitate anchoringimplant 100 to adjacent vertebral bodies following insertion of implant100 between the vertebral bodies. Set of blades 240 may be furthercomprised of first blade 241 and second blade 242. Although theexemplary embodiments described herein include two blades, otherembodiments of an implant could include any other number of blades. Forexample, in another embodiment, three blades could be used. In anotherembodiment, four blades could be used, with two blades extending fromthe inferior surface and two blades extending from the superior surfaceof the implant. Still other embodiments could include five or moreblades. In yet another embodiment, a single blade could be used.

An implant with blades can include provisions for moving the blades withrespect to a housing of the implant. In some embodiments, an implantincludes a blade actuating component that engages with one or moreblades to extend and/or retract the blades from the surfaces of theimplant. In the embodiment shown in FIGS. 4-5, implant 100 includes ablade actuating component 260. In some embodiments, blade actuatingcomponent 260 is coupled to first blade 241 and second blade 242.Moreover, by adjusting the position of blade actuating component 260within housing 201, first blade 241 and second blade 242 can beretracted into, or extended from, surfaces of implant 100.

An implant can include provisions for locking the position of one ormore elements of the implant. In embodiments where the position of ablade actuating component can be changed, an implant can includeprovisions for locking the actuating component in a given position,thereby also locking one or more blades in a given position, such asthrough the use of a threaded fastener or other type of securingmechanism. In the embodiment shown in FIG. 5, implant 100 includeslocking screw 280. In some embodiments, locking screw 280 can be used tolock blade actuating component 260 in place within implant 100, whichensures first blade 241 and second blade 242 remain in an extended ordeployed position, as will be shown further below.

Embodiments can also include one or more fasteners that help attach abody to a cover. In some embodiments, pins, screws, nails, bolts, clips,or any other kinds of fasteners could be used. In the embodiment shownin FIG. 5, implant 100 includes a set of pins 290 that help fasten cover220 to body 200. In the exemplary embodiments, two pins are used,including first pin 291 and second pin 292. In other embodiments,however, any other number of pins could be used. In another embodiment,a single pin could be used. In still other embodiments, three or morepins could be used.

Body Component

Referring now to FIGS. 6-9, four views are presented of an embodiment ofbody 200. FIG. 6 is a schematic isometric superior side or top-downisometric view of body 200. FIG. 7 depicts a schematic isometricinferior side or bottom-up isometric view of body 200. FIG. 8 is aschematic posterior or rear side view of body 200. FIG. 9 is a schematicanterior or front side view of body 200. In different embodiments, body200 may provide the posterior and anterior sides of housing 201, as wellas at least one lateral side of housing 201.

In some embodiments, the lateral sides of a body may both have alattice-like geometry. Various openings or apertures, as will bediscussed below, can help reduce the overall weight of the implant,and/or decrease manufacturing costs associated with material usage.Furthermore, in some cases, openings can increase the surface areaavailable throughout body 200, and facilitate the application of bonegrowth promoting materials to the implant, and/or facilitate thecoupling of the implant with the insertion tool, as will be discussedfurther below. In some other embodiments, the lateral sides could beconfigured as solid walls with one or more openings. Furthermore, byproviding openings in the housing of the implant, there can be improvedvisual clarity regarding the degree or extent of blade deployment.

In the exemplary embodiment shown in FIGS. 6-9, body 200 has a generallyoval cross-sectional shape in a horizontal plane. Furthermore, each ofsuperior side 130 and inferior side 140 include at least onethrough-hole opening. For example, in FIGS. 6 and 7, it can be seen thatimplant 100 includes a first opening 610 and a second opening 612. Eachof first opening 610 and second opening 612 extend continuously throughthe thickness of implant 100 from superior side 130 to inferior side 140in a direction substantially aligned with vertical axis 124. While theopenings can vary in size, shape, and dimension in differentembodiments, in one embodiment both first opening 610 and second opening612 each have a generally half-circle or semi-circle cross-sectionalshape along the horizontal plane.

In addition, as shown in FIGS. 8 and 9, posterior side 112 and anteriorside 110 of body 200 have a generally oblong rectangular shape.Furthermore, in FIGS. 4, 6 and 8-9, it can be seen that a sidewall 630extends around the majority of perimeter of body 200, extending betweensuperior side 130 to inferior side 140 in a direction substantiallyaligned with vertical axis 124, forming a periphery that surrounds ordefines a majority of the outer surface of the implant. In someembodiments, first lateral side 114 and second lateral side 116 aresubstantially similar (i.e., can include substantially similarstructural features), though in other embodiments, each side can includevariations. There may be additional openings formed in implant 100 insome embodiments. In different embodiments, sidewall 630 can include aplurality of side openings or apertures, though in other embodiments,sidewall 630 can be substantially continuous or solid.

Referring back to FIG. 4, it can be seen that first lateral side 114includes a first aperture 480, a second aperture 482, a third aperture484, a fourth aperture 486, a fifth aperture 488, and a sixth aperture490. Each aperture can differ in shape in some embodiments. For example,first aperture 480 has a substantially oblong rectangular shape, secondaperture 482 has a five-sided or substantially pentagonal shape, thirdaperture 484 and fifth aperture 488 each have a four-sided orsubstantially trapezoidal shape, fourth aperture 486 has a substantiallyround shape, and sixth aperture 490 has a six-sided or substantiallyhexagonal shape. In other embodiments, second lateral side 116 caninclude a fewer or greater number of apertures. It should be understoodthat second lateral side 116 can also include a plurality of aperturesdisposed in a similar arrangement as first lateral side 114 in someembodiments. The shapes of the various openings are configured to permitthe implant body to be manufactured in the Direct Metal Laser Sintering(DMLS) process, as well as to provide support to the inferior andsuperior load bearing surfaces.

As shown in FIG. 6, in one embodiment, anterior side 110 of body 200includes guide opening 222. Guide opening 222 extends through thethickness of sidewall 630 in a direction substantially aligned withposterior-anterior axis 122. Guide opening 222 includes a chamberportion (“chamber”) 492 and a hollow grooved portion (the hollow groovedportion will be discussed further below with respect to FIGS. 31 and32). Chamber 492 can be understood to be connected with the groovedportion such that some components can pass from chamber 492 into thegrooved portion (or vice versa).

In some embodiments, as will be discussed further below and is showngenerally in FIG. 4, a portion of blade actuating component 260 can beconfigured to extend through or be received by the chamber portion. Inother words, in some embodiments, the chamber portion can be sized anddimensioned to fit or extend closely around a portion of blade actuatingcomponent 260. In FIG. 6, it can be seen that chamber 492 comprises agenerally oblong four-sided opening. In one embodiment, chamber 492 hasa substantially oblong square or rectangular cross-sectional shape in avertical plane. In FIG. 6, chamber 492 extends between anoutwardly-facing or distally oriented surface 685 of sidewall 630 and aninwardly-facing or proximally oriented surface 695 of sidewall 630. Aschamber 492 approaches proximally oriented surface 695, there may beadditional recessed regions or diagonal slots 632 which expand the sizeof guide opening 222, and can be configured to snugly receive or fitvarious portions of blade actuating component 260, as will be discussedfurther below. Furthermore, it can be understood that thecross-sectional shape of the chamber portion is configured to preventrotation of the driven shaft portion when the drive shaft portion isinserted into the chamber portion.

Body 200 can also include additional reinforcement structures. Forexample, as shown in FIGS. 6 and 7, body 200 includes a first innersidewall 634 extending in a direction substantially aligned withposterior-anterior axis 122 and a second inner sidewall 636 extending ina direction substantially aligned with posterior-anterior axis 122.First inner sidewall 634 and second inner sidewall 636 can besubstantially parallel in one embodiment. As noted above, differentportions of body 200 can include recessed areas or apertures. In oneembodiment, shown best in FIG. 7, first inner sidewall 634 and/or secondinner sidewall 636 include a plurality of apertures 645.

Furthermore, in some embodiments, first inner sidewall 634 and secondinner sidewall 636 can help define or bound a central hollow region 638in body 200. Central hollow region 638 can extend through the thicknessof body 200. Central hollow region 638 can be configured to receive theblades and the blade actuating component, as will be discussed furtherbelow. In FIGS. 6 and 7, it can be seen that central hollow region 638includes a main opening 640 and a posterior opening 642, where mainopening 640 is connected with a posterior opening 642 such that somecomponents can pass from main opening 640 into posterior opening 642.Main opening 640 is located toward a center or middle portion of thebody, and posterior opening 642 is located along the posterior peripheryof the body. In one embodiment, posterior opening 642 is significantlynarrower in width across the horizontal plane relative to the widthassociated with main opening 640.

In different embodiments, posterior opening 642 can be disposed betweena first end portion 696 and a second end portion 698 that are associatedwith posterior side 112 of body 200. Furthermore, in some embodiments,each end portion can include a recessed region. In FIG. 6, a firstposterior recess 692 is formed within a portion of first end portion 696and a second posterior recess 694 is formed within a portion of secondend portion 698. As will be discussed below with respect to FIGS. 20 and21, first posterior recess 692 and second posterior recess 694 can beconfigured to receive a cover.

First end portion 696 and a second end portion 698 can be substantiallysimilar in some embodiments. In one embodiment, first end portion 696and a second end portion 698 are mirror-images of one another relativeto a central posterior-anterior axis or midline. In some embodiments,first posterior recess 692 and second posterior recess 694 are sized anddimensioned to snugly receive a rearward cover or cap that extendsbetween or bridges together first end portion 696 and second end portion698 of body 200, providing a substantially continuous outer periphery ofthe implant. In addition, in some embodiments, either or both of firstend portion 696 and second end portion 698 can include pin holes (shownin FIG. 5 as pin holes 202), which can be used to help secure the coverto the posterior side of body 200 (see FIGS. 20-21).

The configuration of body 200 shown for the embodiment of FIGS. 6-9 mayfacilitate the manufacturing process in different embodiments. Inparticular, this configuration may permit 3D Printing via laser orelectron beam with minimal support structures by forming a unitary piecewith a plurality of openings. This design may also help to improvevisibility of adjacent bony anatomy under X-ray fluoroscopy while stillproviding sufficient structural support and rigidity to withstand alltesting requirements and the clinical loading of an implant. Otherembodiments, not pictured in the figures, include round or rectangularopenings in otherwise solid geometry of the anterior, posterior, orlateral sides.

Embodiments can also include one or more blade retaining portions. Ablade retaining portion may receive any part of a blade, including oneor more edges and/or faces of the blade. In one embodiment, a bodyincludes blade retaining portions to receive the anterior and posterioredges of each blade. As seen in FIG. 6, body 200 includes a first bladeretaining portion 600 positioned toward anterior side 110 of first innersidewall 634 and a second blade retaining portion 602 positioned towardposterior side 112 of first inner sidewall 634. Thus, each bladeretaining portion is formed in an outer perimeter of a lateral side ofmain opening 640 of central hollow region 638. First blade retainingportion 600 comprises a first blade retaining channel extending throughthe depth of body 200 that is configured to receive an anterior edge ofthe first blade (see FIG. 13). Likewise, second blade retaining portion602 comprises a second blade retaining channel extending through thedepth of body 200 that is configured to receive a posterior edge of thefirst blade (see FIG. 13).

In some embodiments, one or more channels can be oriented in a directionthat is substantially diagonal relative to the horizontal plane. In oneembodiment, a channel can be oriented approximately 45 degrees relativeto the horizontal plane. In other embodiments, a channel can be orientedvertically (approximately 90 degrees relative to the horizontal plane)or can be oriented between 30 degrees and 90 degrees relative to thehorizontal plane. The orientation of a channel can be configured tocorrespond to the orientation of the anterior edges and/or posterioredges of a blade in some embodiments.

Body 200 also includes third blade retaining portion 604 and fourthretaining portion 606 for receiving the anterior and posterior edges ofthe second blade. This configuration may help maximize available bonegraft volume within the implant since the lateral edges of the bladesserve as tracks for translation. Specifically, this limits the need foradditional track members on the blade that would take up additionalvolume in the implant. Furthermore, the arrangement of the retainingchannels and the associated blade edges results in most of the volume ofthe retaining channels being filled by the blade edges in the retractedposition, which helps prevent any graft material or BGPM (details on theeffect and use of bone growth promoting material will be discussedfurther below) from entering the retaining channels and inhibitingnormal blade travel.

Blades and Blade Actuating component

FIG. 10 is an isometric side view of an embodiment of blade actuatingcomponent 260. A front or anterior side view of blade actuatingcomponent 260 is also shown in FIG. 11, and a lateral side view of bladeactuating component 260 is depicted in FIG. 12. Referring to FIGS.10-12, blade actuating component 260 may include a driven shaft portion320 and a blade engaging portion 322. Driven shaft portion 320 furtherincludes a driven end 262 along the anterior-most end of driven shaftportion 320.

In some embodiments, driven end 262 can include one or more engagingfeatures. For example, driven shaft portion 320 can include a threadedopening 267 that is accessible from driven end 262, as best seen in FIG.10. In some embodiments, threaded opening 267 may receive a tool with acorresponding threaded tip. With this arrangement, driven end 262 can betemporarily mated with the end of a tool (see FIG. 37) used to impactblade actuating component 260 and drive the set of blades into adjacentvertebrae. This may help keep both the driving tool and driven end 262aligned during the impact, as well as reduce the tendency of the drivingtool to slip with respect to driven end 262. Using mating features alsoallows driven end 262 to be more easily “pulled” distally from implant100, which can be used to retract the blades, should it be necessary toremove the implant or re-position the blades.

In addition, driven shaft portion 320 can be substantially elongatedand/or narrow relative to blade engaging portion 322. For example, inFIGS. 10 and 12, driven shaft portion 320 is seen to comprise asubstantially elongated rectangular prism. In other words, driven shaftportion 320 has a substantially rounded rectangular cross-sectionalshape in the vertical plane. Furthermore, as best seen in FIG. 12, bladeengaging portion 322 has a greater width in the direction aligned withvertical axis 124, and includes a generally rectangular shape with aU-shaped or wrench shaped posterior end. The size and shape of bladeactuating component 260 allows driven shaft portion 320 to smoothlyinsert into the guide opening formed in of the body (see FIG. 6) whileblade engaging portion 322 is shaped and sized to be positioned in thecentral opening of the body (see FIG. 7) and configured to receive theblade set.

Furthermore, as will be discussed further below with respect to FIGS. 20and 21, blade actuating component 260 includes provisions for securingor receiving a portion of the cover within the implant. For example, inFIGS. 10 and 12, blade actuating component 260 includes an actuatingposterior end 1200, which includes a receiving portion 1210. Receivingportion 1210 can be sized and dimensioned to receive, fit, or bedisposed around a portion of the cover in some embodiments. In oneembodiment, receiving portion 1210 comprises a mouth 1220 with twoprongs that are spaced apart from one another along vertical axis 124.In some cases, the two prongs can be spaced apart by a width that issubstantially similar to the thickness of the cover.

A blade actuating component can include provisions for coupling with oneor more blades. In some embodiments, a blade actuating component caninclude one or more channels. In the exemplary embodiment of FIGS. 10and 11, blade engaging portion 322 includes a first channel 350 and asecond channel 352. First channel 350 may be disposed in a first sidesurface 334 of blade actuating component 260 while second channel 352may be disposed in a second side surface 336 of blade actuatingcomponent 260.

In addition, referring to FIG. 11, it can be seen that blade engagingportion 322 is oriented diagonally with respect to vertical axis 124. Inother words, a superior end 342 of blade engaging portion 322 is offsetwith respect to an inferior end 344, such that the two ends are notaligned relative to vertical axis 124 when viewed from the anterior sideof the component. In some embodiments, this can allow first channel 350and second channel 352 to be approximately aligned in the verticaldirection.

FIG. 13 is a schematic isometric view of a distal face 408 of firstblade 241, FIG. 14 is a schematic isometric view of a proximal face 410of first blade 241, and FIG. 15 depicts an inferior side 1330 of firstblade 241. First blade 241, or simply blade 241, includes an outer edge400 associated with inferior side 1330 of blade 241, an inner edge 402associated with a superior side 1340, an anterior edge 404 and aposterior edge 406. These edges bind distal face 408 (i.e., a faceoriented in the outwardly-facing or distal direction) and proximal face410 (i.e., a face oriented in the inwardly-facing or proximaldirection).

In different embodiments, the geometry of a blade could vary. In someembodiments, a blade could have a substantially planar geometry suchthat the distal face and the proximal face of the blade are eachparallel with a common plane, as best shown in FIG. 15. In otherembodiments, a blade could be configured with one or more bends. In someembodiments, a blade can have a channel-like geometry (ex. “C”-shaped or“S”-shaped). In the embodiment shown in FIG. 15, blade 241 has aU-shaped geometry with flanges. In particular, blade 241 a first channelportion 420, a second channel portion 422 and a third channel portion424. Here, the first channel portion 420 is angled with respect tosecond channel portion 422 at a first bend 430. Likewise, third channelportion 424 is angled with respect to second channel portion 422 atsecond bend 432. Additionally, blade 241 includes a first flange 440extending from first channel portion 420 at a third bend 434. Blade 241also includes a second flange 442 extending from third channel portion424 at a fourth bend 436. This geometry for blade 241 helps provideoptimal strength for blade 241 compared to other planar blades of asimilar size and thickness, and allowing for greater graft volume.

Furthermore, in some embodiments, blade 241 can include provisions forincreasing the support or structural strength of blade 241. In oneembodiment, blade 241 includes a bridge portion 1350 that is disposed orformed on distal face 408. Referring to FIG. 13, bridge portion 1350extends between third bend 434 and fourth bend 436. Bridge portion 1350can be configured to increase the structural support of blade 2412. Indifferent embodiments, bridge portion 1350 can include features thatprovide a truss, brace, buttress, strut, joist, or other type ofreinforcement to the curved or undulating structure of blade 241. In oneembodiment, bridge portion 1350 is disposed nearer to the inner edgerelative to the outer edge, such that bridge portion 1350 is offsetrelative to the distal face of the blade.

In some embodiments, bridge portion 1350 includes a relatively wideU-shaped or curved V-shaped outer sidewall 1370. In FIG. 13, outersidewall 1370 extends between third bend 434 and fourth bend 436.Furthermore, bridge portion 1350 can have an inner sidewall (disposed onthe opposite side of the bridge portion relative to the outer sidewall)that is disposed flush or continuously against the distal surfaces offirst channel portion 420, second channel portion 422, and third channelportion 424, represented in FIG. 13 by a U-shaped edge 1380. In oneembodiment, the U-shape associated with the inner sidewall or edge ofbridge portion 1350 is substantially similar to the U-shape geometry ofblade 241.

Bridge portion 1350 can also be substantially symmetrical in someembodiments. For example, in FIG. 13, bridge portion 1350 comprises afirst triangular prism portion 1310 joined to a second triangular prismportion 1320 by a central curved portion. Each portion can bolster thestructure of the blade, and provide resistance against the pressuresapplied to a blade by external forces during use of the implant. Thus,bridge portion 1350 can improve the ability of blade 241 to resistexternal pressures and forces and/or help maintain the specific shape ofblade 241.

In the exemplary embodiment, the outer edge 400 is a penetrating edgeconfigured to be implanted within an adjacent vertebral body. Tomaximize penetration, outer edge 400 may be sharpened so that blade 241has an angled surface 409 adjacent outer edge 400. Moreover, in someembodiments, anterior edge 404 and posterior edge 406 are also sharpenedin a similar manner to outer edge 400 and may act as extensions of outeredge 400 to help improve strength and penetration. It can be understoodthat, in some embodiments, bridge portion 1350 can also serve to helpprevent the blades from extending further outward into a vertebraedownward once they reach the desired deployment extension.

A blade can further include provisions for coupling with a bladeactuating component. In some embodiments, a blade can include aprotruding portion. In some embodiments, the protruding portion canextend away from a face of the blade and may fit within a channel in ablade actuating component. Referring to FIG. 14, blade 241 includes aprotruding portion 450 that extends from proximal face 410. Protrudingportion 450 may generally be sized and shaped to fit within a channel ofthe blade actuating component (i.e., first channel 350 shown in FIG.11). In particular, the cross-sectional shape may fit within a channelof the blade actuating component. In some cases, the cross-sectionalwidth of protruding portion 450 may increase between a proximal portion452 and a distal portion 454 allowing protruding portion 450 to beinterlocked within a channel as discussed in detail below.

A protruding portion may be oriented at an angle on a blade so as to fitwith an angled channel in a blade actuating component. In the embodimentof FIG. 14, protruding portion 450 may be angled with respect to inneredge 402 such that the body of blade 241 is vertically oriented withinthe implant when protruding portion 450 is inserted within the firstchannel. In other words, the longest dimension of protruding portion 450may form a protruding angle 459 with inner edge 402.

Although the above discussion is directed to first blade 241, it may beappreciated that similar principles apply for second blade 242. Inparticular, in some embodiments, second blade 242 may have asubstantially identical geometry to first blade 241. Furthermore, whilereference is made to a superior side and inferior side with respect tothe first blade, it will be understood that, in some embodiments, theorientation of the second blade can differ such that the inner edge isassociated with the inferior side and the outer edge is associated withthe superior side.

As noted above, each blade may be associated with the blade engagingportion of the blade actuating component. In FIG. 16, an explodedisometric view is shown with blade actuating component 260, first blade241, and second blade 242, and in FIG. 17, first blade 241 and secondblade 242 are assembled within blade actuating component 260. It can beseen that protruding portion 450 of first blade 241 fits into firstchannel 350. Likewise, protruding portion 455 of second blade 242 fitsinto second channel 352. Referring to FIGS. 16 and 17, blade engagingportion 322 may comprise a superior surface 330, an inferior surface332, a first side surface 334, and a second side surface 336. Here,first side surface 334 may be a first lateral side facing surface andsecond side surface 336 may be a second lateral side facing sidesurface.

Each channel that is formed in blade engaging portion 322 is seen toextend at an angle between superior surface 330 and inferior surface 332of blade engaging portion 322. For example, as best seen in FIG. 16,first channel 350 has a first end 354 open along superior surface 330and a second end 356 open along inferior surface 332. Moreover, firstend 354 is disposed further from driven shaft portion 320 than secondend 356. Likewise, second channel 352 includes opposing ends on superiorsurface 330 and inferior surface 332, though in this case the enddisposed at superior surface 330 is disposed closer to driven shaftportion 320 than the end disposed at inferior surface 332.

In different embodiments, the angle of each channel could be selected toprovide proper blade extension for varying implant sizes. As usedherein, the angle of a channel is defined to be the angle formed betweenthe channel and a transverse plane of the blade actuating component. Inthe embodiment of FIGS. 16 and 17, first channel 350 forms a first anglewith transverse plane 370 of blade actuating component 260, while secondchannel 352 forms a second angle with transverse plane 370. In theexemplary embodiment, the first angle and the second angle are equal toprovide balanced reactive forces as the blades are deployed. Byconfiguring the blades and blade actuating component in this manner,each blade is deployed about a centerline (e.g., transverse plane 370)of the blade actuating component, which helps minimize friction andbinding loads between these parts during blade deployment. Additionally,the arrangement helps provide balanced reaction forces to reduceinsertion effort and friction.

In different embodiments, the angle of each channel could vary. In someembodiments, a channel could be oriented at any angle between 15 and 75degrees. In other embodiments, a channel could be oriented at any anglebetween 35 and 65 degrees. Moreover, in some embodiments, the angle of achannel may determine the angle of a protruding portion in acorresponding blade. For example, protruding angle 459 formed betweenprotruding portion 450 and inner edge 402 of blade 241 (see FIG. 14) maybe approximately equal to the angle formed between first channel 350 andtransverse plane 370. This keeps the outer penetrating edge of blade 241approximately horizontal so that the degree of penetration does not varyat different sections of the blade.

Furthermore, as seen in FIG. 16, each channel has a cross-sectionalshape that facilitates a coupling or fit with a corresponding portion ofa blade. As an example, channel 350 has an opening 355 on first sidesurface 334 with an opening width 390. At a location 357 that isproximal to opening 355, channel 350 has a width 392 that is greaterthan opening width 390. This provides a cross-sectional shape forchannel 350 that allows for a sliding joint with a corresponding part offirst blade 241. In the exemplary embodiment, first channel 350 andsecond channel 352 are configured with dovetail cross-sectional shapes.In other embodiments, however, other various cross-sectional shapescould be used that would facilitate a similar sliding joint connectionwith a correspondingly shaped part. In other words, in otherembodiments, any geometry for a blade and a blade actuating componentcould be used where the blade and blade actuating component includecorresponding mating surfaces of some kind. In addition, in someembodiments, blade engaging portion 322 may be contoured at the superiorand inferior surfaces to resist subsidence and allow maximum bladedeployment depth. This geometry may also help to keep the blade engagingportion 322 centered between vertebral endplates. As an example, thecontouring of superior surface 330 and inferior surface 332 in thepresent embodiment is best seen in the enlarged cross-sectional view ofFIG. 17.

Each channel may be associated with a first channel direction and anopposing second channel direction. For example, as best seen in FIG. 10,first channel 350 may be associated with a first channel direction 460that is directed towards superior surface 330 along the length of firstchannel 350. Likewise, first channel 350 includes a second channeldirection 462 that is directed towards inferior surface 332 along thelength of first channel 350.

With first protruding portion 450 of first blade 241 disposed in firstchannel 350, first protruding portion 450 can slide in first channeldirection 460 or second channel direction 462. As first protrudingportion 450 slides in first channel direction 460, first blade 241 movesvertically with respect to blade actuating component 260 such that firstblade 241 extends outwardly on a superior side of the implant to adeployed position (see FIGS. 26-27). As first protruding portion 450slides in second channel direction 462, first blade 241 moves verticallywith respect to blade actuating component 260 such that first blade 241is retracted within housing 201 of implant 100 (see FIG. 28). In asimilar manner, second protruding portion 455 of second blade 242 mayslide in first and second channel directions of second channel 352 suchthat second blade 242 can be extended and retracted from implant 100 onan inferior side (see FIGS. 25-28). By using this configuration, bladeactuating component 260 propels both blades in opposing directionsthereby balancing the reactive loads and minimizing cantilevered loadsand friction on the guide bar.

As shown in the cross section of FIG. 17, the fit between each blade andthe respective channel in blade actuating component 260 may beconfigured to resist motion in directions orthogonal to thecorresponding channel directions. For example, with first protrudingportion 450 inserted within first channel 350, first blade 241 cantranslate along first channel direction 460 or second channel direction462, but may not move in a direction 465 that is perpendicular to firstchannel direction 460 and second channel direction 462 (i.e., blade 241cannot translate in a direction perpendicular to the length of firstchannel 350). Specifically, as previously mentioned, the correspondingcross-sectional shapes of first channel 350 and first protruding portion450 are such that first protruding portion 450 cannot fit through theopening in first channel 350 on first side surface 334 of bladeactuating component 260.

In some embodiments, each protruding portion forms a sliding dovetailconnection or joint with a corresponding channel. Using dovetail trackson the blade actuating component and corresponding dovetail features onthe posterior and anterior blades allows axial movement along the angleof inclination while preventing disengagement under loads encounteredduring blade impaction and retraction. For example, in FIG. 17, firstprotruding portion 450 forms a sliding dovetail joint with first channel350. Of course, the embodiments are not limited to dovetail joints andother fits/joints where the opening in a channel is smaller than thewidest part of a protruding portion of a blade could be used.

It may be appreciated that in other embodiments, the geometry of theinterconnecting parts between a blade and a blade actuating componentcould be reversed. For example, in another embodiment, a blade couldcomprise one or more channels and a blade actuating component couldinclude corresponding protrusions to fit in the channels. In suchembodiments, both the protruding portion of the blade actuatingcomponent and the channels in the blades could have correspondingdovetail geometries.

Body and Cover

As discussed above with respect to FIG. 5, embodiments of implant 100can include a cover 220 that is configured to close or bridge theposterior opening of body 200 and help secure the various components ofimplant 100 together. FIG. 18 is a schematic isometric superior-sideview of an embodiment of cover 220, and is a schematic isometricinferior-side view of an embodiment of cover 220. Referring to FIGS. 18and 19, cover 220 includes one or more openings for engaging differentparts of implant 100. For example, cover 220 may include a first pinhole 227 and a second pin hole 228 that are configured to receive afirst pin and a second pin, respectively (see FIG. 5). Each pin hole cancomprise a through-hole that extends from the superior surface to theinferior surface of cover 220, though in other embodiments pin holes canbe blind holes. Moreover, first pin hole 227 and second pin hole 228(shown in FIGS. 18 and 19) of cover 220 may be aligned withcorresponding holes in the body, as discussed below.

FIG. 20 is a schematic isometric exploded view of body 200 and cover220. FIG. 21 is a schematic isometric assembled view of body 200 andcover 220, together forming housing 201 of implant 100. Specifically, insome embodiments, cover 220 can be inserted into the recesses associatedwith a posterior end 2000 of body 200. In addition, first pin hole 227and second pin hole 228 shown in FIG. 20 can be aligned with the pinreceiving openings of body 200 comprising between two and fourthrough-hole channels in posterior end 2000. In FIG. 20, first endportion 696 includes a third pin hole 2030 in a superior portion offirst end portion 696 and a fourth pin hole 2040 in an inferior portionof first end portion 696. Similarly, second end portion 698 includes afifth pin hole 2050 in a superior portion of second end portion 698 anda sixth pin hole 2060 in an inferior portion of second end portion 698.When cover 220 is received by body 200, as shown in FIG. 21, third pinhole 2030 and the fourth pin hole are aligned with the first pin hole ofcover 220, and fifth pin hole 2050 and the sixth pin hole are alignedwith the second pin hole of cover 220. Other embodiments may have afewer or greater number of pin holes. In some embodiments, body 200 mayonly include third pin hole 2030 and fifth pin hole 2050, for example.Once cover 220 has been inserted into body 200, first pin 291 and secondpin 292 (see FIG. 20) can be inserted into the two sets of pin holes tofasten or secure the body to the cover.

Insertion Position and Deployed Position of Implant

As noted above, the embodiments described herein provide an implant thatcan move from a first position (the “insertion position”), which allowsthe implant to maintain a low profile, to a second position (the“impaction position” or the “deployed position”), that deploys theblades and inserts them into the proximal superior and inferiorvertebral bodies. While the implant is in the first (insertion)position, the blades of the device may be retracted within the body ofthe implant (i.e., the blades may themselves be in a “retractedposition”). In the second (deployed) position of the implant, the bladesextend superiorly (or cranially) or inferiorly (or caudally) beyond theimplant and into the vertebral bodies to prevent the implant from movingout of position over time. Thus, the blades themselves may be said to bein an “extended position” or “deployed position”. When the blades aredeployed, the implant resists left to right rotation and resists flexionand/or extension. It may be appreciated that although the blades mayapproximately move in vertical directions (i.e., the superior andinferior directions), the actual direction of travel may vary from oneembodiment to another. For example, in some embodiments the blades maybe slightly angled within the implant and may deploy at slight anglesrelative to a vertical direction (or to the inferior/superiordirections).

FIGS. 4, 21, and 22-24 illustrate several views of implant 100 indifferent operating modes or operating positions. Specifically, FIG. 4is a schematic isometric anterior side view of implant 100 in aninsertion position. FIG. 21 is a schematic isometric posterior side viewof implant 100 in the same insertion position of FIG. 4. Referring toFIG. 4, in the insertion position, driven end 262 of blade actuatingcomponent 260 may be disposed distal to the chamber portion of body 200(i.e., a portion of blade actuating component 260 is disposed or extendsthrough the chamber portion). With implant 100 in the insertionposition, first blade 241 and second blade 242 are retracted withinhousing 201. Thus, as best seen in FIGS. 4 and 21, neither first blade241 or second blade 242 extend outwardly (distally) from superior side130 or inferior side 140, respectively, of implant 100. In thisinsertion position, implant 100 has a compact profile and can be moreeasily maneuvered into place in the excised disc space between adjacentvertebrae.

FIG. 22 is a schematic isometric view of implant 100 in a deployedposition. FIG. 23 is a schematic anterior side view of implant 100 inthe same deployed position of FIG. 22. FIG. 24 is a schematic lateralside view of implant 100 in the same deployed position of FIG. 23.Referring to FIG. 23, in the deployed position, driven end 262 of bladeactuating component 260 may be disposed proximally to an anterioropening 2250 formed in the outer periphery of body 200 (i.e., theentirety of blade actuating component 260 is disposed within implant100). With implant 100 in the deployed position, first blade 241 andsecond blade 242 are extended outwards from superior side 130 andinferior side 140, respectively, so as to be inserted into adjacentvertebral bodies. Furthermore, each blade remains positioned in thecentral hollow region of the body in both the retracted and extendedpositions. For example, an inner edge of each blade is disposed in acentral hollow region of the housing in the retracted position, and theinner edge of the blade remains in the central hollow region in theextended position.

In some embodiments, one or more blades could be deployed at a slightangle, relative to the normal directions on the superior and inferiorsurfaces of the implant. In some embodiments, one or more blades couldbe oriented at an angle between 0 and 30 degrees. In other embodiments,one or more blades could be oriented at an angle that is greater than 30degrees. In the exemplary embodiment shown in FIG. 23, first blade 241and second blade 242 are both oriented at a slight angle from normalaxis 251. Specifically, first blade 241 forms a first angle 250 withnormal axis 251 and second blade 242 forms a second angle 252 withnormal axis 251. In one embodiment, first angle 250 and second angle 252are both approximately 10 degrees. Angling the blades in this way mayhelp keep first blade 241 and second blade 242 approximately centered inthe adjacent vertebrae upon deployment. In an exemplary embodiment, thecommon anterior implant blade angle is chosen to keep the blades closeto the centerline of the vertebral body to minimize rotational loads onthe vertebral bodies during blade deployment and also to provide anoptional cover plate screw clearance. In addition, it can be seen inFIG. 23 that the outer edge of each blade is positioned toward a centralregion of the implant when the blade is deployed, such that the outeredge is positioned centrally relative to the housing in the extendedposition.

The extension of each blade could vary in different embodiments. In someembodiments, a blade could extend outwardly by a length between 0 and100% of the depth of an implant. In still other embodiments, combinedblade height could extend outwardly by a length between 100 and 130% ofthe depth of an implant. In the exemplary embodiment shown in FIGS.22-24, first blade 241 and second blade 242 combined may be coverable ofextending outwardly from implant 100 by an amount equal to 110% of thedepth of implant 100. This can be done while still keeping the bladesfully retracted within implant 100 since the blades are guided by tworobust parallel tracks in body 200 and also by angled cross channels inblade actuating component 260, thus constraining all six axes of motion.In other embodiments, the combined blade height at deployment could beless than 100%. In one embodiment, the implant could be designed so thatthe combined blade height is less than 10 mm to reduce the risk offracturing the adjacent vertebral bodies. In another embodiment, theimplant has a combined blade height of 6 mm or less.

Furthermore, as disclosed in the “Implant With Deployable Blades”application, in some embodiments, implant 100 can use a three-pointattachment configuration for each of first blade 241 and second blade242. Specifically, each blade is received along its lateral edges by twoblade retaining portions, and also coupled to blade actuating component260 using the dovetail connection described above. In other words,anterior edge 404 of first blade 241 is received within the first bladeretaining channel of first blade retaining portion 600. Posterior edge406 of first blade 241 is received within a second retaining channel ofsecond blade retaining portion 602. Moreover, distal face 408 of firstblade 241 remains unattached to any other elements of implant 100. Notonly does first blade 241 remain unattached along distal face 408, butthe entirety of distal face 408 between anterior edge 404 and posterioredge 406 is spaced apart from (i.e., not in contact with) all otherelements of implant 100. Further, second blade 242 is likewise attachedat its lateral edges to corresponding blade retaining portions and alsocoupled to blade actuating component 260 using a sliding dovetailconnection. Thus, first blade 241 and second blade 242 are held inimplant 100 using a three-point attachment configuration that may limitunwanted friction on first blade 241 and second blade 242 duringimpaction. It may be appreciated that the fit between each blade andeach blade retaining channel may provide sufficient clearance to allowfor translation of the blades along the retaining channels. In otherwords, the fit may not be so tight as to impede movement of the lateraledges within the retaining channels.

In different embodiments, the cross-sectional geometry of channels inone or more blade retaining portions could vary. In some embodiments,the cross-sectional geometry could be rounded. In the embodimentsdisclosed herein, first blade retaining portion 600 (see FIG. 22) has arectangular blade retaining channel. This rectangular geometry for theblade tracks or channels and tolerance allows for precise axial travelwithout binding from actuation ramp angular variations. In someembodiments, the posterior edge and anterior edge of each blade mayremain in the tracks or channels of each blade retaining portion whilethe blades are retracted to prevent bone graft material from restrictingfree deployment of the blades.

Using an interlocking joint, such as a dovetail sliding joint, toconnect the blades and a blade actuating component helps prevent theblades from decoupling from the blade actuating component during impact.Additionally, with an interlocking joint the blade actuating componentcan be used to retract the blades.

FIGS. 25-28 illustrate several schematic views of implant 100 during animpact sequence (FIGS. 25-27) as well as during a step of retracting theblades (FIG. 28). In FIGS. 25-28, housing 201 of implant 100 is shown inphantom to better show blade actuating component 260, first blade 241and second blade 242. Also, each of FIGS. 25-28 include cross-sectionalviews of a section of blade actuating component 260, first blade 241 andsecond blade 242 to better illustrate the coupling between these partsduring actuation.

In FIG. 25, implant 100 is in the insertion position, with first blade241 and second blade 242 fully retracted within housing 201. Next, asseen in FIG. 26, an impacting force 700 is applied to driven end 262 ofblade actuating component 260. As blade actuating component 260 istranslated towards posterior side 112 of implant 100, blade actuatingcomponent 260 applies forces to first blade 241 and second blade 242along first channel 350 and second channel 352, respectively.Specifically, the orientation of first channel 350 is such that firstblade 241 is forced towards the inferior side of implant 100. Likewise,the orientation of second channel 352 is such that second blade 242 isforced towards the superior side of implant 100. However, in otherembodiments, the channel orientations can be switched such that firstblade 241 is forced towards the inferior side of implant 100 and secondblade 242 is forced towards the superior side of implant 100.

Furthermore, the interlocking connection between first protrudingportion 450 and first channel 350 (as well as between second protrudingportion 455 and second channel 352) means that both blades remaincoupled to the motion of blade actuating component 260 at all times. Itshould be noted that since both blades are restricted from moving in alongitudinal direction, the resulting motion of each blade is purelyvertical. Moreover, using the dovetail shaped protruding portions foreach blade means the protruding portions are both lifting at the centerline to limit any cocking force or rotational moments that could resultin increased (friction) resistance to motion or binding of these movingparts.

Using this configuration, the forces deploying the blades are balancedthrough the blade actuating component 260 in order to minimize frictionand binding between driven shaft portion 320 and the guide opening inbody 200 (see FIG. 6), which helps to guide blade actuating component260 and keep its motion restricted to directions parallel to thelongitudinal axis (see FIG. 2).

In FIG. 27, implant 100 has been placed in the fully deployed position,with both first blade 241 and second blade 242 fully extended fromimplant 100. As seen in the cross-sectional view, both first blade 241and second blade 242 remain coupled with blade actuating component 260when implant 100 is in the fully deployed position. Because of thiscoupling, the motion of blade actuating component 260 can be reversed toretract first blade 241 and second blade 242, as shown in FIG. 28.

It may be appreciated that in some embodiments a blade actuatingcomponent (e.g., blade actuating component 260) may function to supportadjacent vertebral bodies. This is can be accomplished by using a bladeactuating component with a height similar to the height of the outersupport structure so that the superior and inferior surfaces of theblade actuating component may come into contact with the vertebralbodies following implantation. Since the blade actuating componentfunctions as a load bearing structure within the implant, this may freeup additional space in the implant otherwise occupied by additionalsupport structures, thereby increasing the internal volume available forbone graft or BGPMs.

Referring to FIG. 28, driven end 262 of blade actuating component 260may be pulled in an opposing direction to the motion shown in FIG. 26.For example, in some embodiments a delivery tool can be coupled todriven end 262 using a threaded connector. Then, as the tip of thedelivery tool is retracted a retracting or pulling force 710 may beapplied to drive end 262. As blade actuating component 260 (andspecifically, blade engaging portion 322) is pulled towards anteriorside 110 of implant 100, blade actuating component 260 applies forces tofirst blade 241 and second blade 242 along first channel 350 and secondchannel 352, respectively. Specifically, the orientation of firstchannel 350 is such that first blade 241 is forced towards the superiorside of implant 100. Likewise, the orientation of second channel 352 issuch that second blade 242 is forced towards the inferior side ofimplant 100. Although not shown, applying sufficient force at driven end262 may result in full retraction of first blade 241 and second blade242 so that implant 100 is returned to the insertion position shown inFIG. 25.

As noted above, body 200 may include guide opening 222 that receives aportion of blade actuating component 260. When the implant is in thedeployed position, the driven shaft portion can be disposed securely inthe chamber portion. In some embodiments, the chamber portion of guideopening 222 may have a shape that matches the cross-sectional shape of adriven shaft portion of a blade actuating component. In someembodiments, both the chamber portion and the driven shaft portion ofthe blade actuating component have rectangular cross-sectional shapes(see FIGS. 9 and 11). This configuration may allow axial motion, butcontrol rotational and angular loads that could result during bladeimpaction.

Locking Screw

FIGS. 29 and 30 illustrate two schematic views of locking screw 280,according to an embodiment. Locking screw 280 can be a type of threadedfastener in some embodiments. In FIG. 29, locking screw 280 includes aflanged head 282 with a threaded segment portion 284 and furtherincludes a substantially smooth and elongated body portion 288. Threadedsegment portion 284 is sized and dimensioned to engage with the groovedportion of the body (see FIG. 33 below). Flanged head 282 can alsoinclude a receiving recess 2900 which can engage with a driving tool inorder to secure the locking screw within the implant. Thus, althoughbody portion 288 is disposed within threaded opening of the bladeactuating component when the screw lock is secured, body portion 288need not engage or lock with the threading associated with the threadedopening.

Implant 100 can include provisions for securing the implant 100 in thedeployed position. Referring to the exploded isometric view of FIG. 31,guide opening 222 can include a grooved portion 3100 that is formeddirectly adjacent to the chamber portion. Grooved portion 3100 can havea round cross-sectional shape in the vertical plane, and has a widerdiameter relative to the diameter or width of the chamber portion. Thediameter of grooved portion 3100 can be configured to mate with thediameter of the flanged head. In one embodiment, grooved portion 3100 isdisposed directly adjacent to the outermost anterior periphery of guideopening 222. As locking screw 280 is inserted into the anterior side ofguide opening 222 (see FIG. 32), threaded segment portion 284 thatextends around flanged head 282 of locking screw 280 can engage withgrooved portion 3100, securing locking screw 280 to body 200. When inthis position, body portion 288 of locking screw 280 can also bedisposed through the passageway of threaded opening 267 of bladeactuating component 260. As shown best in the partial cross-sectionalview of FIG. 32, when implant 100 is in the deployed position, a portionof driven shaft portion 320 is disposed within chamber 492 of guideopening 222, primarily comprising the portion of driven shaft portion320 that includes threaded opening 267. Furthermore, flanged head 282 oflocking screw 280 extends from anterior opening 2250 through groovedportion 3100, and body portion 288 of locking screw 280 extends throughthreaded opening 267 of driven shaft portion 320. Flanged head 282 isprevented from moving further into guide opening 222 because of thelarger diameter of flanged head 282 relative to body portion 288. Thus,it can be understood that the insertion of the implant and thedeployment of the blades of the implant occur through the engagement ofan insertion tool within only a single guide opening 222, improvingsurgical efficiency and safety.

Alternate Blade Actuating Component

In different embodiments, an implant can utilize different types ofcomponents to provide the features and functions described herein. Insome embodiments, the features of blade actuating component can beadjusted in order to facilitate the use of implant with a variety ofsurgical requirements. For example, in some embodiments, an alternateembodiment of a second blade actuating component (“second actuatingcomponent”) 3300 can be placed within the housing of the body, as shownin FIG. 33. In FIG. 33, second actuating component 3300 is configuredwith a receiving portion 3350 with a mouth 3320 that is greater in widththan the embodiment of the actuating blade component presented above.Adjustments to the size of a mouth in the receiving portion of a bladeactuating component can correspond to changes in the dimensions or shapeof a cover, bridge piece, or cap that is used in the implant.

In addition, to allow an implant to withstand varying forces and workwith different blade types, the height and/or other dimensions of theblade engaging portion can be increased or decreased. For example, inFIG. 12, blade actuating component 260 has a first maximum height 1230,and in FIG. 33, second actuating component 3300 has a second maximumheight 3330. First maximum height 1230 is less than second maximumheight 3330, such that blade actuating component 260 can be insertedinto a smaller region of the human body. However, when the blades beingused must be increased in size, the greater height of second actuatingcomponent 3300 provides the structural support to the device. Inaddition, second actuating component 3300 includes diagonal portions3340 disposed toward the center of the actuating component that canextend the length of channels 3310 and support additional blade weight.In some embodiments, diagonal portions 3340 are integrally formed withsecond actuating component 3300. In addition, diagonal portions 3340 canadd a curved or sloped interface to the actuating component relative toblade actuating component described earlier (see FIG. 12) in which theintersection between drive shaft portion 320 and blade engaging portion322 is substantially perpendicular.

In order to provide greater detail with respect to the initial insertionposition and the deployed position, FIGS. 34 and 35 provide twocross-sectional views of the implant prior to the application of animpacting force (see FIG. 26) and subsequent to the application of theimpacting force. It should be noted that while FIGS. 34 and 35 employsecond actuating component 3300, the general operation and transitionfrom insertion to deployment of implant 100 remains substantially thesame to the process described above with respect to blade actuatingcomponent 260. In FIG. 34, second actuating component 3300 is disposedsuch that driven end 262 extends distally outward and away from ananterior end 3400 of body 200. The remainder of second actuatingcomponent 3300 is positioned such that it is offset relative to theinterior space of the implant along posterior-anterior axis 122. Inother words, the majority of blade engaging portion 322 is disposednearer to anterior end 3400 than to posterior end 2000 of body 200 inthe insertion position.

However, when an impacting force is applied to driven end 262, thesubstantial entirety of second actuating component 3300 can be disposedwithin the internal space of the body. Furthermore, actuating posteriorend 1200 can move translationally from the main opening of the centralhollow region in body 200 toward the posterior opening. It can be seenthat a portion of posterior opening 642 is filled with or bridged by acentral portion of cover 220. As actuating posterior end 1200 approachesthe posterior opening, receiving portion 1210 comprising the two-prongedmouth shown in FIG. 33 can slide or be positioned above the superiorsurface and below the inferior surface of cover 220, helping to securethe assembly in place and forming a continuous outer surface.

Furthermore, as noted above, in FIG. 34 it can be seen that threadedopening 267 of driven shaft portion 320 can be configured to receive athreaded driving tool. In addition, as shown in FIG. 35, threadedflanged head 282 of the locking screw engages with grooved portion 3100formed in the structure of body 200, and the locking screw body issmoothly inserted within the channel provided by threaded opening 267.Driven end 262 can be positioned directly adjacent to the posterior endof grooved portion 3100 when implant 100 is in the deployed position. Inother words, once implant 100 is in the deployed position, driven end262 is disposed such that it is spaced apart from the outer openingformed in body 200 by the region comprising grooved portion 3100.

Insertion Process

As noted above, embodiments of implant 100 can make use of features orstructures disclosed in the “Insertion Tool For Implant And Methods ofUse” application. In some embodiments, implant 100 can be configured foruse with a single tool that can significantly facilitate theimplantation process. For example, whether a surgeon approaches the discspace from an anterior approach can be dependent on how comfortable thesurgeon is with the anterior approach and operating around the aorta andvena cava. By approaching a patient from the anterior side, there can bea risk of vessel injury, as the aorta and vena cava lie in front of thespine. However, the benefits of added stability and fusion area veryoften outweigh the risks of the extra surgery, and the process ofdeployment provided herein can help lower such risks.

In some embodiments, body 200 may include attachment points for aninsertion instrument. In FIGS. 36 and 37, a portion of an insertion tool3600 is shown with implant 100. In FIG. 36, insertion tool 3600 is shownas it holds or grasps implant 100. In FIG. 37, the same view of FIG. 36is shown in a partial cross-section to reveal the engagement of athreaded driver 3610 in guide opening 222.

Body 200 may include provisions for interacting with insertion tool3600. For example, as seen in FIG. 37, body 200 may include a firstcavity 580 and a second cavity 582 (where first cavity 580 refers tofirst aperture 480 as identified in FIG. 6). Each of first cavity 580and second cavity 582 may receive the ends of an insertion tool 3600 toimprove the grip of the tool on implant 100 during insertion into (orremoval from) between the vertebrae of the spine. Furthermore, the sameinsertion tool 3600 can be utilized to transition implant 100 from theinsertion position to the deployed position. As shown in FIGS. 36 and37, insertion tool 3600 can be used to grasp the implant body. While theimplant body is grasped by two gripping jaws 3620, the blade actuatingcomponent can be controlled and/or driven by threaded driver 3610. Thisarrangement can maintain the blades in a retracted position duringimplant insertion and transfers the impact loads from the surgeon whenthe threaded cover is removed from the proximal end. Thus, the insertionstep, deployment step, and locking screw insertion step can occurthrough the use of a single tool, and through interaction primarily withonly the anterior facing side of the implant. Furthermore, as bladeactuating component is pushed inward or outward, there is rotationassociated with the threaded driver. The use of insertion tool 3600 andthe single guide opening 222 allows the rotation to be generallyenclosed or shielded within the jaws of the insertion tool. This processcan serve to reduce the risks associated with the insertion of variousforeign objects into the patient.

Implant Dimensions

In different embodiments, the size of an implant could vary. In someembodiments, an implant could have any length. Embodiments could havelengths ranging from 40 mm to 60 mm. In some cases, a manufacturer couldprovide multiple implant options with lengths varying between 40 mm and60 mm in 5 mm increments. In some embodiments, an implant could have anyheight. Embodiments could have a height ranging from 4 mm to 16 mm. Insome cases, a manufacturer could provide implants with heights varyingfrom 4 mm to 16 mm in 2 mm increments. Embodiments could have widths(i.e., size along the posterior-anterior axis) of 18 mm, 22 mm, 26 mm aswell as other sizes.

Embodiments can also be constructed with various lordosis angles, thatis, angles of incline between the posterior and anterior sides.Embodiments could be configured with lordosis angles of 8, 15 and 20degrees, for example. In other embodiments, other lordosis angles couldbe used for an implant. Furthermore, in some embodiments, the blades canbe angled to accommodate additional implants or other implanted devicein the spine that are located at adjacent levels, fosteringstabilization in the patient's system.

Alignment Features

Embodiments may optionally include one or more alignment features.Exemplary alignment features include, but are not limited to, windowsfor fluoroscopy positioning, windows for blade deployment validation,windows for aligning a blade actuating component with one or moreblades, as well as various other kinds of alignment features. Referringto FIG. 4, body 200 of implant 100 includes a central alignment window(referred to as fourth aperture 486 in FIG. 4). Additionally, as shownin FIG. 13, blade 241 includes an alignment window 297. Alignment window297 may align with the central alignment window when blade 241 is fullyretracted. Moreover, blade actuating component 260 includes an actuatingalignment window 277, as shown in FIG. 12. Actuating alignment window277 may align with the implant body center line when the first blade andthe second blade are fully deployed or fully retracted. One or more ofthese windows (i.e., the central alignment window or actuating alignmentwindow 277) may also facilitate fluoroscopy positioning and may be usedto confirm blade deployment. For example, in some cases, when the firstblade and the second blade are fully deployed, the blades may clearactuating alignment window 277 of blade actuating component 260.

In some embodiments, the dovetail connections can help to more preciselycontrol the blade position in both directions. Some embodiments of theimplant may also include one or more stroke limiting stops. For example,there may be two stroke limiting stops formed on blade actuatingcomponent 260. These stops may help prevent over travel of bladeactuating component 260. Specifically, a stroke limiting stop maycontact the internal surfaces of body 200. In other words, the bladeactuating component has a limited stroke dictated by the length of itsdistal portion and the inside depth of the implant, measured from theinside of the implant proximal wall and the inside surface of the coverthat is pinned in place.

Materials

The various components of an implant may be fabricated frombiocompatible materials suitable for implantation in a human body,including but not limited to, metals (e.g. titanium, titanium alloy,stainless steel, cobalt-chrome, or other metals), synthetic polymers(e.g. PEEK or PEKK), ceramics, and/or their combinations, depending onthe particular application and/or preference of a medical practitioner.

Generally, the implant can be formed from any suitable biocompatible,non-degradable material with sufficient strength. Typical materialsinclude, but are not limited to, titanium, biocompatible titanium alloys(e.g. Titanium Aluminides (including gamma Titanium Alum inides),Ti₆—Al₄—V ELI (ASTM F 136 and ASTM F 3001), or Ti₆—Al₄—V (ASTM F 1108,ASTM F 1472, and ASTM F 2989) and inert, biocompatible polymers, such aspolyether ether ketone (PEEK) (e.g. PEEK-OPTIMA®, Invibio Inc, Zeniva®,Solvay Inc., or others). Optionally, the implant contains a radiopaquemarker to facilitate visualization during imaging when constructed ofradiolucent biomaterials.

In different embodiments, processes for making an implant can vary. Insome embodiments, the entire implant may be manufactured and assembledvia traditional and CNC machining, injection-molding, cast or injectionmolding, insert-molding, co-extrusion, pultrusion, transfer molding,overmolding, compression molding, 3-Dimensional (3-D) printing,dip-coating, spray-coating, powder-coating, porous-coating, milling froma solid stock material and their combinations.

In one embodiment, body 200 may be produced by Additive Manufacturing.Specifically, Direct Metal Laser Sintering (DMLS) using powder Ti-6Al-4VELI, and then traditional or CNC machined in specific locations toprecise dimensions. Moreover, in one embodiment, as shown in FIG. 5,blade actuating component 260, first blade 241, second blade 242, cover220, pins 290 and locking screw 280 may also be made of a materialincluding titanium.

Implantation

Some embodiments may use a bone growth promoting material, includingbone graft or bone graft substitute material. As used herein, a “bonegrowth promoting material” (BGPM) is any material that helps bonegrowth. Bone growth promoting materials may include provisions that arefreeze dried onto a surface or adhered to the metal through the use oflinker molecules or a binder. Examples of bone growth promotingmaterials are any materials including bone morphogenetic proteins(BMPs), such as BMP-1, BMP-2, BMP-4, BMP-6, and BMP-7. These arehormones that convert stem cells into bone forming cells. Furtherexamples include recombinant human BMPs (rhBMPs), such as rhBMP-2,rhBMP-4, and rhBMP-7. Still further examples include platelet derivedgrowth factor (PDGF), fibroblast growth factor (FGF), collagen, BMPmimetic peptides, as well as RGD peptides. Generally, combinations ofthese chemicals may also be used. These chemicals can be applied using asponge, matrix or gel.

Some bone growth promoting materials may also be applied to animplantable prosthesis through the use of a plasma spray orelectrochemical techniques. Examples of these materials include, but arenot limited to, hydroxyapatite, beta tri-calcium phosphate, calciumsulfate, calcium carbonate, as well as other chemicals.

A bone growth promoting material can include, or may be used incombination with a bone graft or a bone graft substitute. A variety ofmaterials may serve as bone grafts or bone graft substitutes, includingautografts (harvested from the iliac crest of the patient's body),allografts, demineralized bone matrix, and various synthetic materials.

Some embodiments may use autograft. Autograft provides the spinal fusionwith calcium collagen scaffolding for the new bone to grow on(osteoconduction). Additionally, autograft contains bone-growing cells,mesenchymal stem cells and osteoblast that regenerate bone. Lastly,autograft contains bone-growing proteins, including bone morphogenicproteins (BMPs), to foster new bone growth in the patient.

Bone graft substitutes may comprise synthetic materials includingcalcium phosphates or hydroxyapatites, stem cell containing productswhich combine stem cells with one of the other classes of bone graftsubstitutes, and growth factor containing matrices such as INFUSE®(rhBMP-2-containing bone graft) from Medtronic, Inc.

It should be understood that the provisions listed here are not meant tobe an exhaustive list of possible bone growth promoting materials, bonegrafts or bone graft substitutes.

In some embodiments, BGPM may be applied to one or more outer surfacesof an implant. In other embodiments, BGPM may be applied to internalvolumes within an implant. In still other embodiments, BGPM may beapplied to both external surfaces and internally within an implant.

While various embodiments have been described, the description isintended to be exemplary, rather than limiting, and it will be apparentto those of ordinary skill in the art that many more embodiments andimplementations are possible that are within the scope of theembodiments. Although many possible combinations of features are shownin the accompanying figures and discussed in this detailed description,many other combinations of the disclosed features are possible. Anyfeature of any embodiment may be used in combination with, orsubstituted for, any other feature or element in any other embodimentunless specifically restricted. Therefore, it will be understood thatany of the features shown and/or discussed in the present disclosure maybe implemented together in any suitable combination. Accordingly, theembodiments are not to be restricted except in light of the attachedclaims and their equivalents. Also, various modifications and changesmay be made within the scope of the attached claims.

What is claimed is:
 1. An implant, comprising: a housing, the housinghaving a first axis; a blade, the blade having a retracted position inthe housing and an extended position where the blade extends outwardlyfrom the housing; a blade actuating component, the blade actuatingcomponent comprising a driven shaft portion and a blade engagingportion; wherein the blade actuating component can move the bladebetween the retracted position and the extended position; the housingincluding a first end, the first end including a guide opening, theguide opening comprising a hollow grooved portion and a chamber portion,the hollow grooved portion being connected to the chamber portion; andthe chamber portion receiving a portion of the driven shaft portion ofthe blade actuating component; and
 2. The implant according to claim 1,wherein the chamber portion is configured to receive the driven shaftportion, and wherein the cross-sectional shape of the chamber portion isconfigured to prevent rotation of the driven shaft portion.
 3. Theimplant according to claim 1, wherein the chamber portion has asubstantially rectangular cross-sectional shape in a vertical plane, andwherein the driven shaft portion has a substantially rectangularcross-sectional shape in the vertical plane.
 4. The implant according toclaim 1, wherein the first axis extends between an anterior side to aposterior side of the implant.
 5. The implant according to claim 4,wherein the first end is associated with the anterior side of theimplant.
 6. The implant according to claim 1, wherein the bladeactuating component can translate through the housing in directionsparallel to the first axis.
 7. The implant according to claim 1, whereinthe hollow grooved portion is configured to receive a threaded fastener.8. The implant according to claim 7, wherein the threaded fastenerincludes a flanged head portion joined to a body portion, wherein theflanged head portion includes a threaded segment, wherein the threadedsegment corresponds to a threading of the hollow grooved portion.
 9. Theimplant according to claim 7, wherein the threaded fastener isconfigured to prevent the driven end from moving from the chamberportion into the hollow grooved portion.
 10. An implant, comprising: abody, the body having a first axis; a blade, the blade having aretracted position in the body and an extended position where the bladeextends outwardly from the body; the blade also having a distal face anda proximal face; the blade further comprising a bridge portion disposedadjacent to the distal face, the bridge portion being configured toprovide structural reinforcement to the blade; a blade actuatingcomponent that can translate through the body in directions parallel tothe first axis; and wherein the blade actuating component can move theblade between the retracted position and the extended position.
 11. Theimplant according to claim 10, wherein the blade has an anterior edgeand a posterior edge, wherein the body includes a first retainingchannel and a second retaining channel, wherein the anterior edge of theblade is received in the first retaining channel and wherein theposterior edge of the blade is received in the second retaining channel.12. The implant according to claim 10, wherein the blade has a firstbend where a first blade portion and a second blade portion meet at anonzero angle.
 13. The implant according to claim 10, wherein aposterior side of the body includes a posterior opening extendingbetween a first end portion and a second end portion, and wherein acover is attached to the body to bridge the posterior opening.
 14. Theimplant according to claim 13, wherein the first end portion includes afirst recess configured to receive a portion of the cover.
 15. Theimplant according to claim 14, wherein a posterior end of the bladeactuating component includes a receiving portion, and wherein thereceiving portion is disposed above a superior surface of the cover andbelow an inferior surface of the cover when the cover is attached to thebody and the blade is in the retracted position.
 16. The implantaccording to claim 10, wherein the channel in the blade actuatingcomponent extends diagonally on a side of the blade actuating component.17. An implant, comprising: a housing, a first blade, and a bladeactuating component; the first blade having a retracted position in thehousing and an extended position where the first blade extends outwardlyfrom the housing; the blade actuating component configured to translatethrough the housing in directions parallel to a first axis, the firstaxis extending from an anterior side of the implant to a posterior sideof the implant; and the blade actuating component comprising a drivenshaft portion and a blade engaging portion, the driven shaft portionbeing disposed at least partially outside of the housing when the firstblade is the retracted position, the driven shaft portion being disposedentirely within the housing when the first blade is in the extendedposition.
 18. The implant according to claim 17, wherein the drivenshaft portion includes a threaded opening extending in a directionsubstantially aligned with the first axis.
 19. The implant according toclaim 17, wherein the housing includes an anterior opening formed in ananterior side of the housing, wherein the driven shaft portion extendsthrough the anterior opening when the first blade is in the retractedposition.
 20. The implant according to claim 19, wherein the anteriorside of the housing includes at least a first cavity configured toengage with an insertion tool.
 21. The implant according to claim 17,further comprising a second blade, the first blade extending distallyupward from the housing in the extended position and the second bladeextending distally downward from the housing in the extended position.22. The implant according to claim 21, wherein the second blade issubstantially similar to the first blade.
 23. The implant according toclaim 18, wherein an insertion tool is configured to grip the housingduring insertion of the implant, wherein the insertion tool furthercomprises a threaded driver that engages with the threaded opening totransition the first blade from the retracted position to the extendedposition, and wherein the insertion tool includes a threaded fastenerthat is secured to the implant to lock the first blade in the extendedposition.
 24. The implant according to claim 17, wherein the bladeactuating component includes a diagonal portion disposed toward a centerof the blade actuating component.
 25. The implant according to claim 17,wherein the driven shaft portion includes a driven end that is disposedoutside of the housing when the blade is in the retracted position, andwherein the blade transitions from the retracted position to theextended position when a force is applied to the driven end portion. 26.The implant according to claim 25, wherein an outer edge of the blade isdisposed in a central region of the housing in the retracted position,and wherein the outer edge of the blade is positioned centrally relativeto the housing in the extended position.